Diacutaneus Fibrolysis on Tempromandibular Joint Pain and Trismus Post Oral Surgery

Cairo University (CU)

Status: Completed

Conditions: Temporomandibular Pain

Treatments: Device: Diacutaneus fibrolysis; Device: Transcutaneous electrical nerve stimulation; Procedure: Massage

Study type: Interventional

Funder types: Other

Identifiers

NCT06675149

012/005335

Details and patient eligibility

About

This study is carried out on sixty patients who will have tempromandibular pain and trismuspostOral and Maxillofacial Surgeryand their ages will be ranged from 18 to 40 years.

Enrollment: 60 patients

Sex: All

Ages: 18 to 40 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Ages of patients will be ranged from 18 to 40 years.
2. All patients will have Oral and Maxillofacial Surgery.
3. All patients will be referred by a surgeon before starting the study procedure.
4. All participants will have pain and trismus in the jaw,
5. The participants will be also cleared for periodontal issues.
6. All patients will enter the study having their informed consent

Exclusion criteria

1. Patients with associated vascular injuries requiring arterial repair.
2. Patient with systemic diseases such as arthritis; pain attributable to confirmed migraine, head, or neck pain condition
3. Patient with acute infection or other significant disease of the teeth, ears, eyes, nose, or throat
4. Patient with present neurologic or cognitive deficit.
5. Patients with history of previously failed surgeries.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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60 participants in 2 patient groups, including a placebo group

Group B

Experimental group

Description:

This group includes 30 patients who will receive 4 weeks(3times/week) DiacutaneusFibrolysis in addition to post-surgical traditional physiotherapy .

Treatment:

Procedure: Massage

Device: Transcutaneous electrical nerve stimulation

Device: Diacutaneus fibrolysis

Group A

Placebo Comparator group

Description:

This group will includes 30 patients who will receive 4 weeks (3times/week) post-surgical traditional physiotherapy (TENS , massage , range of motion exercise ) .

Treatment:

Procedure: Massage

Device: Transcutaneous electrical nerve stimulation